Abstract
Abstract Accurate values for the orientation-averaged long-range dipole-dipole dispersion energy coefficients, C 6(A, B), have been determined for all possible pair interactions involving ground state H, Li, N, O, H2, N2, O2, NH3, H2O, NO, and N2O. The calculations have been carried out by employing dipole oscillator strength distributions for these species that have been constructed (except in the case of H) by using discrete oscillator strength, photo-absorption, and high energy inelastic scattering data and by requiring the distributions to reproduce the Thomas-Reiche-Kuhn sum rule and, in the case of the molecules, available accurate refractivity and dispersion measurements for the relevant dilute gases. These oscillator strength distributions were also used to evaluate the refractivity R(λ), as a function of wavelength λ in the visible and ultra-violet region below the ultra-violet absorption thresholds, and the dipole oscillator strength sums S -2l , l = 1, 2, …, 7, for each atom and molecule. The calculated values of R(λ) provide refractivities for wavelengths, especially in the ultra-violet region, for which accurate experimental data are often not available. The accurate results for C 6(A, B) and for various dipole oscillator strength sums are used to make self-consistent tests of the adequacy of (1) the C 6(A, A) bounds provided by Padé approximant methods and (2) various semi-empirical formulae for C 6(A, B). Some problems that can arise in using other procedures to evaluate the S -2l and C 6(A, B) are discussed briefly. This research was supported by a grant from the National Research Council of Canada and by grant 240 of the Ontario Cancer Treatment Research Foundation. This research was supported by a grant from the National Research Council of Canada and by grant 240 of the Ontario Cancer Treatment Research Foundation. Notes This research was supported by a grant from the National Research Council of Canada and by grant 240 of the Ontario Cancer Treatment Research Foundation. Additional informationNotes on contributorsG.D. Zeiss Associated with the Centre for Interdisciplinary Studies in Chemical Physics. William J. Meath Associated with the Centre for Interdisciplinary Studies in Chemical Physics.
Keywords
Affiliated Institutions
Related Publications
A Chemically Functionalizable Nanoporous Material [Cu <sub>3</sub> (TMA) <sub>2</sub> (H <sub>2</sub> O) <sub>3</sub> ] <sub> <i>n</i> </sub>
Although zeolites and related materials combine nanoporosity with high thermal stability, they are difficult to modify or derivatize in a systematic way. A highly porous metal c...
Epidemiology of Sporadic Diarrhea Due to Verocytotoxin-Producing Escherichia coli: A Two-Year Prospective Study
Journal Article Epidemiology of Sporadic Diarrhea Due to Verocytotoxin-Producing Escherichia coli: A Two-Year Prospective Study Get access Chik H. Pai, Chik H. Pai Department of...
Can the Clusters Zr<sub>6</sub>O<sub>4</sub>(OH)<sub>4</sub>(OOCR)<sub>12</sub> and [Zr<sub>6</sub>O<sub>4</sub>(OH)<sub>4</sub>(OOCR)<sub>12</sub>]<sub>2</sub> Be Converted into Each Other?
Abstract Upon reaction of zirconium alkoxides, Zr(OR) 4 , with carboxylic acids, the clusters Zr 6 O 4 (OH) 4 (OOCR) 12 ( Zr6 ) or [Zr 6 O 4 (OH) 4 (OOCR) 12 ] 2 ( Zr12 ) were o...
In<sub>2</sub>(OH)<sub>3</sub>(BDC)<sub>1.5</sub> (BDC = 1,4-Benzendicarboxylate): An In(III) Supramolecular 3D Framework with Catalytic Activity
The new hybrid inorganic-organic polymer In(2)(OH)(3)[O(4)C(8)H(4)](1.5) has been hydrothermally obtained. Conditions for the synthesis are reported. The crystal structure of th...
Optical Absorption Intensities of Rare-Earth Ions
Electric dipole transitions within the $4f$ shell of a rare-earth ion are permitted if the surroundings of the ion are such that its nucleus is not situated at a center of inver...
Publication Info
- Year
- 1977
- Type
- article
- Volume
- 33
- Issue
- 4
- Pages
- 1155-1176
- Citations
- 314
- Access
- Closed
External Links
Social Impact
Social media, news, blog, policy document mentions
Citation Metrics
Cite This
Identifiers
- DOI
- 10.1080/00268977700100991